Novel benzotriazole derivatives and organic electroluminescent devices using the derivatives

Active Publication Date: 2014-12-25
HODOGAYA KAGAKU IND
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0030]The benzotriazole derivative of the invention represented by the above general formula (1) is a novel compound and has a benzotriazole ring and a pyridine ring. The benzotriazole derivative having the above structure features the following properties.
[0031]Owing to its stability in the thin-film state, the benzotriazole derivative of the present invention can be used as an organic layer that is provided between the electrodes of an organic electroluminescent device, and imparts the following properties to the organic EL device.
[0032]For instance, the organic EL device forming the electron injection layer and/or the electron-transporting layer by using the benzotriazole derivative of the invention, features a high electron injection/migration rate, an improved electron transport efficiency from the electron-transporting layer into the luminous layer and, therefore, features a high luminous efficiency, a low driving voltage and a large durability.
[0033]Further, the organic EL device having a hole-blocking layer formed by using the benzotriazole derivative of the invention features excellent hole-blocking power and electron transpo

Problems solved by technology

Here, however, the hole migration rate is higher than the electron migration rate arousing a problem of a decrease in the efficiency since the holes partly pass through the luminous layer.
Tris (8-hydroxyquinoline) aluminum (hereinafter abbreviated as Alq3) which is a representative luminous material has also been generally used as an electron-transporting material having, however, a low electron mobility and a work function of 5.6 eV and, therefore, having a hole-locking capability which is far from satisfactory.
The BCP,

Method used

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  • Novel benzotriazole derivatives and organic electroluminescent devices using the derivatives
  • Novel benzotriazole derivatives and organic electroluminescent devices using the derivatives
  • Novel benzotriazole derivatives and organic electroluminescent devices using the derivatives

Examples

Experimental program
Comparison scheme
Effect test

example 1

Synthesis of a 5-(10-phenyl-anthracen-9-yl)-2-{4-(pyridin-3-yl)phenyl}-2H-benzotriazole (synthesis of a compound 4)

[0139]

1-Bromo-4-nitrobenzene50g,3-Pyridineboronic acid31.9g,2M Potassium carbonate aqueous solution309ml,Toluene200ml,Ethanol40ml, andTetrakistriphenylphosphine palladium (0)11.0g,

were put into a reaction vessel purged with nitrogen, and were heated and refluxed for 14 hours with stirring. The reaction solution was concentrated and the precipitated crystals were picked up by filtration. Through the dispersion washing with an isopropanol, there was obtained a grey powder of 3-(4-nitrophenyl)pyridine crystals in an amount of 43.5 g (yield, 88.80).

The thus obtained 3-(4-nitrophenyl)pyridine3.5 g,4-Bromo-1,2-diaminobenzene3.6 g,Caustic soda1.4 g, andToluene 50 ml,

were put into the reaction vessel purged with nitrogen, and were heated and refluxed for 7 hours with stirring.

[0140]100 Milliliters of toluene was added thereto to extract the reaction solution which was then conc...

example 2

Synthesis of a 5-(10-phenyl-anthracen-9-yl)-2-{3-(pyridin-4-yl)phenyl}-2H-benzotriazole (synthesis of a compound 5)

[0145]

[0146]A 5-bromo-2-{3-(pyridin-4-yl)phenyl}-2H-benzotriazole was synthesized from a 1-bromo-3-nitrobenzene and a pyridin-4-ylboronic acid in the same manner as in Example 1.

The above 5-bromo-2-{3-(pyridin-4-yl)phenyl}-2.9 g,2H-benzotriazole9-Phenylanthracen-10-ylboronic acid2.6 g,2M Potassium carbonate aqueous solution 12 ml,Toluene 30 ml,Ethanol5.6 ml, and

[0147]Tetrakistriphenylphosphine palladium (0) 0.4 g, were put into the reaction vessel purged with nitrogen, and were heated and refluxed for 7.5 hours with stirring.

[0148]The organic layer was picked up by the separating operation, concentrated under a reduced pressure and was refined by the column chromatography to obtain 1.7 g of a yellow powder of 5-(10-phenyl-anthracen-9-yl)-2-{3-(pyridin-4-yl)phenyl}-2H-benzotriazole (compound 5) (yield, 38.7%).

[0149]The obtained yellow powder was identified for its struct...

example 3

Synthesis of a 5-{10-naphthalen-1-yl)anthracen-9-yl}-2-{4-(pyridin-3-yl)phenyl}-2H-benzotriazole (synthesis of a compound 8)

[0151]

The above 5-bromo-2-{4-(pyridin-3-yl)phenyl}-4.0 g,2H-benzotriazole synthesized in Example 110-(Naphthalen-1-yl)anthracen-9-ylboronic acid4.8 g,2M Potassium carbonate aqueous solution 17 ml,Toluene 28 ml, andEthanol  7 ml,

were put into the reaction vessel purged with nitrogen, and through which the nitrogen gas was flown for 60 minutes with stirring.

[0152]Next, 0.7 g of the tetrakistriphenylphosphine palladium (0) was added thereto, and the mixture was heated and refluxed for 10.5 hours with stirring. The organic layer was picked up by the separating operation, concentrated under a reduced pressure and was refined by the column chromatography to obtain 3.5 g of a yellow powder of 5-{10-(naphthalen-1-yl)anthracen-9-yl)-2-{4-(pyridin-3-yl)phenyl}-2H-benzotriazole (compound 8) (yield, 53.5%).

[0153]The obtained yellow powder was identified for its structure b...

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Abstract

Benzotriazole derivatives represented by the following general formula (1),
wherein Ar1 and Ar2 are, for example, aromatic hydrocarbon groups or aromatic heterocyclic ring groups, and A is a group including a pyridine ring. The compounds excel in electron injection/transport capability, feature a high hole-blocking power and a high stability in their thin-film form, and are useful as materials for producing highly efficient and highly durable organic electroluminescent devices.

Description

FIELD OF THE INVENTION[0001]This invention relates to novel benzotriazole derivatives. More specifically, the invention relates to novel benzotriazole derivatives into which a pyridine ring structure has been introduced and to organic electroluminescent devices that have an organic layer containing the above derivatives between the electrodes.BACKGROUND ART[0002]An organic electroluminescent device (hereinafter often called organic EL device) is a spontaneously luminous device which features higher brightness and higher legibility than those of the liquid crystal devices enabling vivid display to be attained and has, therefore, been vigorously studied.[0003]In 1987, C. W. Tang et al. of the Eastman Kodak Co. have developed a device of a layer-laminated structure comprising various kinds of materials to bear individual roles, and have put an organic EL device using organic materials into a practical use. The above organic EL device is constituted by laminating layers of a fluorescent...

Claims

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Application Information

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IPC IPC(8): H01L51/00H01L51/50
CPCH01L51/0058H01L51/0067H01L51/5012H01L51/0052H01L51/0072C07D401/04C07D401/10C07D401/14C09K11/06C09K2211/1059H10K85/615H10K85/626H10K85/654H10K85/6572H10K50/11
Inventor YOKOYAMA, NORIMASANUMAZAWA, SHIGETAKAIRISA, SHIROUHAYASHI, SHUICHI
Owner HODOGAYA KAGAKU IND
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